In the previous papers 1)2) concerning the synthesis of muscarines, we reported a partially stereospecific synthesis in which the hydroxyl group of a diacid (I) was introduced selectively in trans manner to the methyl group. Decarboxylation of I, however , proceeded non-stereoselectively giving a m
The resolution of DL-muscarine
✍ Scribed by C. A. Salemink; H. C. Cox
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 399 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The Debije‐Scherrer diagram of “natural” L(+)‐muscarine‐di‐p‐toluyl‐hydrogen‐D(−)‐tartrate‐hemihydrate is compared with the diagrams of muscarine‐di‐p‐toluyl‐hydrogen‐D(−)‐tartrates resulting from the resolution of two DL‐muscarine preparations. One of the latter diagrams proved to be identical with the diagram of “natural” L(+)‐muscarine‐di‐p‐toluyl‐hydrogen‐D(−)‐tartrate‐hemihydrate whereas the other was entirely different.
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